JP2003183657A - Liquid crystal medium - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a liquid crystal display for a matrix liquid crystal (MLC), a twisted nematic (TN) or a super twisted nematic (STN) display having preferred characteristics. <P>SOLUTION: This liquid crystal medium is based on a mixture of polar compounds having positive dielectric anisotropy. The liquid crystal medium comprises one or more kinds of compounds represented by general formula I (wherein, X is fluorine; ring A is trans-1,4-cyclohexylene or 1,4-phenylene; and R is an alkyl, an oxaalkyl, a fluoroalkyl or an alkenyl having ≤7 carbon atoms in each case) and one or more kinds of compounds selected from the group consisting of general formulas V to VI (wherein, R is an alkyl, an oxaalkyl, a fluoroalkyl or an alkenyl having ≤7 carbon atoms in each case; and Z is -C<SB>2</SB>H<SB>4</SB>-, -CO-O- or -O-CO-). <P>COPYRIGHT: (C)2003,JPO

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to liquid crystal media, their use for electro-optical purposes and displays containing the media.

[0002]

Liquid crystals are used as a dielectric in display devices because they can influence the optical properties of their materials by the application of voltage.
Liquid crystal based electro-optical devices are very familiar to the person skilled in the art and can be based on various effects. Devices of this type are, for example, cells with a dynamic scattering effect, DAP [deformation of aligned p
hases)] cells, guest / host cells, TN cells having a twisted nematic structure, STN [super-twisted nematic] cells, SBE [super-birefringence effect] cells and OM.
I [optical mode interferenc
e)] cell. The most common display device is based on the Schadt-Helfrich effect and has a twisted nematic structure.

Liquid crystal materials must have good chemical and thermal stability and good stability to electric fields and electromagnetic radiation. Furthermore, the liquid crystal material should have a low viscosity and give a short addressing time, a low threshold voltage and a high contrast in the cell. In addition, the liquid crystal material should have suitable mesophases at the normal operating temperature, ie above and below room temperature and as broad as possible, for example nematic or cholesteric mesophases for the cells mentioned above. Since liquid crystals are commonly used as a mixture of components, it is important that the components be readily miscible with each other. Still other properties such as electrical conductivity, dielectric anisotropy and optical anisotropy must meet different requirements depending on the cell type and field of application. For example, materials for cells having a twisted nematic structure should have positive dielectric anisotropy and low conductivity.

For example, desirable media for matrix liquid crystal displays (MLC displays) containing integrated non-linear elements for switching individual image points have high positive dielectric anisotropy, wide nematic phase, relatively low birefringence, It has a very high resistivity, good UV and temperature stability of the resistivity, and a low vapor pressure.

Matrix liquid crystal displays of this kind are known. An example of a non-linear element that can be used to switch each individual image point is an active element (ie a transistor). Therefore, this is called "active matrix", and there are two types, namely 1. 1. MOS (metal oxide semiconductor) transistor on a silicon wafer as a substrate Thin film transistor (TF) on a glass plate as a substrate
T) can be distinguished.

The use of single crystal silicon as the substrate material limits the size of the display because even the modular assembly of various partial displays causes problems at the joints.

For the preferred, more promising type 2, T
The N effect is commonly used as the electro-optic effect. A distinction is made between two technologies, namely TFTs made of compound semiconductors such as CdSe and TFTs based on polycrystalline or amorphous silicon. The latter technology is being researched worldwide with intense fierce intensity.

The TFT matrix is attached to the inside of one glass plate of the display, the other glass plate carrying a transparent counter electrode inside it. Since the TFT is very small compared to the size of the image point electrode, it hardly affects the image. This technique can also be extended to full color image display with mosaic red, green and blue filters arranged such that each filter element is located opposite a switchable image element.

TFT displays usually act as transmissive TN cells with crossed polarizers and are illuminated from behind.

The term MLC display is used herein for any matrix display with integrated non-linear elements, ie active matrix plus varistors or diodes (MIM = metal-insulator-
It also includes a display having a passive element such as metal.

This kind of MLC display is especially suitable for TVs.
Applications (eg, pocket television sets) or for computers (laptops) and high information content displays in automobile or aircraft construction. In MLC displays, in addition to problems with angular dependence of contrast and response time, various problems arise due to insufficient resistivity of the liquid crystal mixture [TOGASHI, S., SEKIGUCHI, K. , TANABE, H., YAMAMOTO, E., SORIMACHI, K., TAJIMA, E., Watanabe (W
ATANABE), H., Shimizu (SHIMIZU), H., Proc. Eurodisp
lay 84 (September 1984): "A210-288 matrix LCD controlled by a two-stage diode ring.
(A 210-288Matrix LCD Controlled by Double Stage D
iode Rings) ”, 141 pages, Paris; Stromer (ST
ROMER), M., Proc. Eurodisplay 84 (September 1984)
Mon): “Design of thin film transistors for addressing LCD matrix for TVs (Design of
Thin Film Transistors for Matrix Addressing of Tel
evision Liquid Crystal Displays) ”, pp. 145, Paris]. The lower the resistance, the worse the contrast of the MLC display, and the problem of "afterimage erasure" may occur. In general, the resistivity of a liquid crystal mixture decreases over the lifetime of the display due to its interaction with the inner surface of the MLC display, so high (initial) resistance is very important to obtain an acceptable service life. It has hitherto been impossible to achieve very high specific resistances, especially in the case of low-voltage mixtures. Furthermore, it is important that the resistivity not rise as much as possible with increasing temperature and after heating and / or UV exposure. Moreover, in some applications, high birefringence, low threshold voltage, relatively high surface tilt angle to avoid "reverse tilt" domains,
Low viscosities, wide nematic mesolayers and good low temperature stability are required. However, prior art MLC displays do not meet these current requirements.

It has the required birefringence and phase range values for practical use (eg clearing point ≧ 70 ° C.) and a retention value of about 98% under extreme conditions (eg after UV exposure). It has heretofore been possible to produce liquid crystal media having a threshold voltage of about 1.8 volts if desired.

[0013]

Therefore, it has none or only a few of these disadvantages, while at the same time having a very high specific resistance with a wide operating temperature range, a short response time and a low threshold voltage. There is still a great need for MLC displays.

For TN (Schut-Helfrich) cells, a medium that promotes the following advantages in the cell is desirable: -extension of the nematic phase range (especially down to low temperatures) -switchability at very low temperatures (field applications, Automotive, Avionics) -Improved stability to UV light (longer life).

The media obtained from the prior art cannot at the same time obtain these advantages while retaining other parameters.

For super-twisted (STN) cells, media having greater multiplexing and / or lower threshold voltage and / or wider nematic phase range (especially at low temperatures) are desirable. To this end, the latitude of available parameters (clearing point, smectic-
(Nematic transition point or melting point, viscosity, dielectric value, elasticity value)
Is urgently desired to be further expanded.

The object of the present invention is in particular that of the MLC, TN or STN of this kind, which preferably does not have the abovementioned disadvantages, or has only a few, and at the same time has a very high specific resistance and a low threshold voltage. It is to provide a medium for a display.

[0018]

It has now been found that this object can be achieved when the medium according to the invention is used in a display.

Accordingly, the present invention is a liquid crystal medium based on a mixture of polar compounds having a positive dielectric anisotropy, having the general formula I

[0020]

[Chemical 8] (In the formula, X is fluorine, chlorine, CF ₃ , OCF ₃ or OC.
HF ₂ , ring A is trans-1,4-cyclohexylene or 1,4-phenylene, and R is alkyl having up to 7 carbon atoms in each case,
Oxaalkyl, fluoroalkyl or alkenyl) and one or more compounds.

The present invention relates to an electro-optical display containing such a medium (in particular two flat parallel skins forming a cell with a frame, an integrated non-linear for switching individual pixels on said skins). It also relates to devices and STN or MLC displays with a positive dielectric anisotropy and a high resistivity nematic liquid crystal mixture provided in the cell) and to the use of these media for electro-optical purposes.

The liquid crystal mixtures according to the invention facilitate a marked widening of the parameter latitude available.

The medium of the present invention is based on a mixture of polar compounds. These compounds are not known highly polar compounds such as nitriles, but are bonded to each other at 1 or 4 sites directly or via a divalent bridging member, and two compounds are end-bonded to two end groups. It is a medium-polarity compound having a rod-like structure having three or four six-membered carbon rings or heterocycles. One of these terminal groups is a non-polar group such as alkyl, alkoxy, oxaalkyl, dioxaalkyl, alkenyl, fluoroalkyl or fluoroalkenyl, and the other terminal group is, for example, fluorine, chlorine, difluoroalkyl, Highly fluorinated halogenated medium polar groups such as alkyl, alkoxy, alkenyl, alkenyloxy or alkanoyloxy.

The compounds of formula I are representative of this group of moderately polar compounds whose ring structure may also be laterally substituted with halogen, preferably fluorine.

The achievable combination of clearing point, birefringence, viscosity at low temperature, thermal and UV stability and dielectric anisotropy is far superior to existing materials from the prior art.

The requirements of high clearing point, nematic phase at -40 ° C. and high Δε have hitherto been achieved only to an unsatisfactory degree. For example, systems such as ZLI-3119 have comparable clearing points and relatively favorable viscosities, but their Δε is only +3.

The other mixture systems have comparable viscosities and Δε values, but only clearing points in the 60 ° C. range.

The liquid crystal mixture of the present invention has a low viscosity at low temperatures (≤600 at -30 ° C, preferably ≤550 m).
Pa. S; ≤1800 at -40 ° C, preferably ≤
1700 mPa. s), and ≧ 3.5, preferably ≧
Dielectric anisotropy value of 4.0, 65 ° or more, preferably 70 °
It is possible to achieve the above-mentioned high values of clearing point and specific resistance. This means that excellent STN and MLC displays can be obtained.

Of course, by proper selection of the components of the mixture according to the invention, a higher clearing point (eg 9) at a higher threshold voltage while retaining other advantageous properties.
It is also possible to achieve (0 ° or more) or a lower clearing point with a lower threshold voltage. ML of the present invention
The C displays are Gooch and Tarr.
y) [C. H. Gooch and H.C. A. Tally, Electron.
Lett. 10 , pp. 2-4 (1974); H. Gooch and H.C. A. Tally, Appl. Phys., Volume 8, 157
5 to 1584 (1975)] first transmission minimum (fi
rst transmission minimum) is preferable.
For example, at the same threshold voltage as in a similar display, the slope of the characteristic is tight and the low angular dependence of the contrast (German Patent 30 22 818).
In addition to particularly preferred electro-optical properties, such as No.), a lower dielectric anisotropy at the second minimum is sufficient in this case.
As a result, with the mixtures according to the invention it is possible to achieve significantly higher specific resistances in the first minimum than with mixtures containing cyano compounds. The person skilled in the art can produce the birefringence required for the prespecified layer thickness of the MLC display by simply using the usual methods and by appropriate selection of the individual components and their weight proportions.

The viscosity at 20 ° C. is 18 ≦ mPa. s,
Especially ≦ 15 mPa. It is preferably s.

The nematic phase range is preferably at least 70 °, especially at least 80 °. This range preferably extends at least from -30 ° to + 85 °.

[Capacity holding rati
o) ”(HR) [S. Liquid such as Matsumoto
Crystals, 5 , 1320 (1989); Niwa et al., SID proceedings, San Francisco, 198
June 2004, p. 304 (1984); Weber et al., Liquid Crystals, 5 , pp. 1381 (19
1989)], the mixture of the present invention containing a compound of formula I

[0033]

[Chemical 9] It was shown that the decrease in HR with increasing temperature was significantly smaller than that of the similar mixture in which the cyanophenylcyclohexanes were replaced. The UV stability of the mixtures according to the invention is also quite good, ie they show a significantly lower HR reduction on UV exposure.

The threshold voltage V _10/0/20 achieved is generally _≤1.6 volts, preferably in the range 1.4 to 1.6 volts.

The media according to the invention are characterized by a very favorable nematic phase range, in addition to a very favorable elastic constant and a very favorable viscosity, which, in particular when used in TFT displays, bring significant advantages over conventional media.

The medium according to the invention comprises a plurality (preferably 2) of the formula I
One or more) compounds, that is,
The proportion of these compounds is ≧ 25%, preferably ≧ 40%
Is preferred.

Formula I which can be used in the medium of the invention
To XII and the individual compounds of their sub-formulas are known or can be prepared according to known compounds.

The preferred embodiments are shown below: The medium has the general formulas II, III and IV:

[0039]

[Chemical 10] Where each group has the following meanings: R: alkyl, oxaalkyl, fluoroalkyl or alkenyl having in each case up to 7 carbon atoms, Q: —C ₂ H ₄ —, —C ₄ H ₈ - or -CO-O-, X: F, Cl, CF 3, OCF 3 or OCHF _2, Y: H or F, A: trans-1,4-cyclohexylene or 1,4
-Phenylene, further comprising one or more compounds selected from the group consisting of r: 0 or 1).

The medium contains one or more compounds of the formula II and / or III in which r is 0.

The medium has the general formulas V and VI:

[0042]

[Chemical 11] (Wherein, R is as defined in formula II-IV, and Z is _{-C 2 H 4 -, - CO} -O- or -O-CO- in which) one selected from the group consisting of It further contains the above compounds.

The medium is of the general formula VII to XII:

[0044]

[Chemical 12] Further comprising one or more compounds selected from the group consisting of: wherein R, r, X and Y are each, independently of one another, as defined in formulas II-IV.

The proportion of compounds of the formulas I to IV in the total mixture together is at least 50% by weight.

The proportion of compounds of the formula I in the total mixture is 1
It is 0 to 50% by weight.

The proportion of compounds of the formulas II to IV in the total mixture is 30 to 70% by weight.

[0048]

[Chemical 13] Is

[0049]

[Chemical 14] Is.

The medium is of formula II and III or IV
Containing the compound of.

-R is a straight chain alkyl or alkenyl having 2 to 7 carbon atoms.

The medium consists essentially of the compounds of the formulas I-IV.

The media are the following groups:

[0054]

[Chemical 15] It contains further compounds which are preferably selected from

The weight ratio of I: (II + III + IV) is preferably 1: 4 to 1: 1.

The medium consists essentially of a compound selected from the group consisting of the general formulas I to XII.

Even when the proportion of compounds of the formula I mixed with conventional liquid crystal materials, in particular liquid crystal materials containing one or more compounds of the formulas II, III and / or IV, is improved significantly. It was found that a lower threshold voltage was obtained, and at the same time, a broad nematic phase was observed at a low smectic-nematic transition temperature.
The compounds of formulas I-IV are colorless, stable and readily miscible with one another and with other liquid crystal substances.

By choosing a particular compound of formula I, or combining more than one type of compound of formula I, the compounds of the invention are definitely improved for different requirements. The following table shows the effect of various compounds of formula I on the important parameters selected. An increasing number of + signs indicates an increasingly strong influence, 0 indicates no influence, and-indicates that the display parameter is impaired. However, there is always a need to make compromises when improving the LC media, so with proper selection of their concentrations, even compounds that are "-" for one parameter are very handy for developing mixtures.

The preferred medium is the formula A

[0060]

[Chemical 16] Concurrently includes a compound of the formula where R, r, X and Y are as defined in formulas II-IV.

It is preferred that r is 0. X is F, C
1, OCF ₃ or OCHF ₂ is preferred. The following combinations of X and Y are especially preferred.

[0062]

[Table 1] Especially preferred is the combination of a compound of formula I with A (a) being cyclohexylene and X (OCHF ₂ ) with A (a) because of the particularly low birefringence and at the same time a low threshold voltage. Similarly, A (b) and A are cyclohexylene,
And preference is given to compounds I in which X is CF ₃ .

Preferred compounds of formula A

[0064]

[Chemical 17] Is represented by the acronym CUP-nX (.F)

[0065]

[Table 2] The term "alkyl" is intended to include straight-chain and branched alkyl groups having 1 to 7 carbon atoms, especially the straight-chain groups methyl, ethyl, propyl, butyl, pentyl, hexyl and heptyl. . Groups having 2-5 carbon atoms are generally preferred.

The term "alkenyl" is intended to include straight-chain and branched alkenyl groups having 2-7 carbon atoms, especially the straight-chain groups. Particularly, the alkenyl group is C ₂
-C _{7-1E-alkenyl,} C ₄ -C ₇ -3E-alkenyl, C ₅ -C _7-4-alkenyl, C ₆ -C _7-5-alkenyl and C _7-6-alkenyl, in particular C ₂ ~ C ₇
-1E- alkenyl, C ₄ -C ₇ -3E-alkenyl and C ₅ -C _7-4-alkenyl. Examples of preferred alkenyl groups are vinyl, 1E-propenyl, 1E-butenyl, 1E-pentenyl, 1E-hexenyl, 1E-heptenyl, 3-butenyl, 3E-pentenyl, 3E-hexenyl, 3E-heptenyl, 4-pentenyl, 4Z-. Hexenyl, 4E-hexenyl, 4Z-heptenyl, 5-
Hexenyl, 6-heptenyl and the like. Groups having up to 5 carbon atoms are generally preferred.

The term "fluoroalkyl" is preferably a straight-chain group having terminal fluorine, ie fluoromethyl, 2-fluoroethyl, 3-fluoropropyl, 4-
It includes fluorobutyl, 5-fluoropentyl, 6-fluorohexyl and 7-fluoroheptyl. However, it does not exclude fluorine at other positions.

[0068] The term "oxaalkyl" preferably formula _{C n H 2n + 1 -O- (} CH 2) m ( wherein, n and m
Each independently of one another is 1 to 6, or m is 0). n is preferably 1 and m is preferably 1-6.

By appropriately selecting the meanings of R, A, X and Y, the address time, the threshold voltage, the slope of the transmission characteristic, etc. can be changed as desired. For example,
1E-alkenyl groups, 3E-alkenyl groups, 2E-alkenyloxy groups, etc. generally have shorter address times, improved nematic propensity and higher elastic constants k ₃₃ (bend) vs. k ₁₁ (spread) compared to alkyl and alkoxy groups. )
Will give the ratio. 4-Alkenyl groups, 3-alkenyl groups, etc. generally give lower threshold voltages and lower k ₃₃ / k ₁₁ values compared to alkyl and alkoxy groups. Z ¹ or -CH in Z ² ₂ CH ₂ in the formula I 'below - groups would give generally higher values of k ₃₃ / k ₁₁ compared with a simple covalent bond. High k ₃₃ / k ₁₁ values can be used, for example, for flat transmission characteristic slopes [to achieve gray tones] and STN, SB in TN cells twisted by 90 °.
Promotes sharp transmission characteristic slopes (greatly multiplex) in E and OMI cells, and vice versa. What properties are desired for the optimum mixing ratio of the compounds of the formulas I and II + III + IV?
Substantially depends on how the components II and / or IV are selected and how other components may be present. An appropriate mixing ratio within the above range can be easily determined depending on the case.

The total amount of compounds of the formulas I to XII in the mixtures according to the invention is not very important. Thus, the mixture may include one or more other ingredients to optimize various properties. However, the observed effects on addressing time and threshold voltage are generally greater at higher total concentrations of compounds of formulas I-XII.

In a particularly preferred embodiment, the medium according to the invention has the formula II, III, V and / or VII (preferably I) in which X is CF ₃ , OCF ₃ or OCHF _2.
It contains a compound of I and / or III). Formula I
The favorable synergistic effect with the compounds of the above results in particularly advantageous properties.

For STN applications, the medium is X is O
It is preferred to include a compound selected from the group consisting of formulas V-VIII, which is preferably CHF ₂ .

The medium of the present invention has the general formula I ′ having a dielectric anisotropy of −1.5 to +1.5:

[0074]

[Chemical 18] (Wherein R ¹ and R ² are each independently n-alkyl, ω-fluoroalkyl or n-alkenyl having up to 9 carbon atoms, and the rings A ¹ , A ² and A ³ are 1,4-phenylene independently of each other,
2- or 3-fluoro-1,4-phenylene, trans-1,4-cyclohexylene or 1,4-cyclohexenylene, wherein Z ¹ and Z ² are each independently of the other —CH ₂ CH ₂ -, -C≡C-, -CO-O
-, -O-CO- or a single bond, and m is 0,
Component A consisting of one or more compounds of 1 or 2)
May be further included.

Component A is II1 to II7:

[0076]

[Chemical 19] It is preferred to include one or more compounds selected from the group consisting of: wherein R ¹ and R ² are as defined in formula I ′.

Component A is II8-II20:

[0078]

[Chemical 20] (In the formula, R ¹ and R ² are as defined in the formula I ′, and the 1,4-phenylene groups in II 8 to II 17 may be each independently of each other mono- or poly-substituted with fluorine.) It is preferred that it further comprises one or more compounds selected from the group consisting of

Further, the component A is II21 to II25:

[0080]

[Chemical 21] (Wherein R ¹ and R ² are as defined in formula I ′,
The 1,4-phenylene group in II21 to II25 is
It is preferred that it still further comprises, independently of one another, one or more compounds selected from the group consisting of (optionally mono- or poly-substituted with fluorine).

Finally, a preferred mixture of this type comprises components A II26 and II27:

[0082]

[Chemical formula 22] _Where C _t H _{2t + 1} is a straight chain alkyl group having up to 7 carbon atoms and includes one or more compounds selected from the group consisting of:

In some cases, the expression

[0084]

[Chemical formula 23] Where R ¹ and R ² are as defined in formula I ′ and Z ⁰ is a single bond, —CH ₂ CH ₂ —,

[0085]

[Chemical formula 24] It has been found that the addition of the compound (1) is advantageous in suppressing the smectic phase although the resistivity may decrease. In doing so, one of ordinary skill in the art can readily determine what amounts these compounds may be added to achieve the ideal combination of parameters for the application. Usually less than 15%, especially 5 to 1
Use 0%.

III 'and IV':

[0087]

[Chemical 25] Also preferred is a liquid crystal mixture containing one or more compounds selected from the group consisting of: wherein R ¹ and R ² are as defined in formula I ′.

The type and amount of polar compound having positive dielectric anisotropy itself is not critical. One of ordinary skill in the art can select the appropriate materials from a wide variety of known and often commercially available ingredients and substrate mixtures using simple routine experimentation. The medium of the present invention has the formula I ″

[0089]

[Chemical formula 26] (In the formula, Z ¹ , Z ² and m are as defined in the formula I ′, and Q ¹ and Q ² are each independently 1,4-
Phenylene, trans-1,4-cyclohexylene or 3-fluoro-1,4-phenylene, or alternatively ^{one of the} groups Q ¹ and Q ² is trans-1,3-dioxane-2,5-diyl, pyrimidine- 2,5-diyl,
Pyridine-2,5-diyl or 1,4-cyclohexenylene)).

R ⁰ is n-alkyl, n-alkenyl, n-alkoxy or n-oxaalkyl having in each case up to 9 carbon atoms, Y is H or F and X ′ is CN, halogen, CF ₃ , OC
F ₃ or OCHF ₂ . In a preferred embodiment, the medium of the invention for STN or TN has X'is CN
Based on a compound of formula I ″ which is of course, of course, it is also possible to include smaller or larger proportions of other compounds of formula I ″ (X ′ ≠ CN). The for MLC, medium of the invention "preferably contain only up to about 10% nitriles (but Formula I" Formula I contains no nitrites, instead X 'is halogen, CF ₃ , O
Preferably includes a compound of formula I 'is CF ₃ or OCHF _2). These media are preferably based on compounds of the formulas II to XII.

The structure of the STN and MLC displays according to the invention from polarisers, electrode base plates and surface-treated electrodes is in agreement with the usual structure for displays of this kind. The term common structure is in this case interpreted broadly and also covers all derivative and refinement elements of the MLC display, in particular matrix display elements based on poly-Si TFTs or MIMs.

However, the essential difference between the display of the invention and the conventional conventional display based on twisted nematic cells is the choice of liquid crystal parameters in the liquid crystal layer.

The liquid crystal mixtures which can be used according to the invention are prepared in a customary manner. In general, the desired amount of the minor components is conveniently dissolved in the main constituent forming components at elevated temperature. It is also possible to mix the solution of each component with an organic solvent such as acetone, chloroform or methanol, and after thorough mixing, remove the solvent again by distillation, for example.

These dielectrics are known to those skilled in the art and can also contain other additives described in the literature. For example, 0-15% of multicolor dyes or chiral doping agents can be added.

[0095]

The following examples illustrate the invention but do not limit it. Above and below, all temperatures are given in ° C. Percent is weight percent
Is. In the specific examples shown below, the examples of the present invention (the specific examples included in the scope of the claims) include the compounds of the formula VI (CCH-32CF3, CCH-
52CF3) and Examples 27-32, 34, 3
5, 109, 110, 112, 115, 120, 12
4, 128, which are compounds of formula V in addition to formula I (CCH
-3CF3, CCH-5CF3) as Example 1
There are 72.

C is a crystal phase, S is a smectic phase, and S
_B is smectic B phase, N is nematic phase and I
Represents an isotropic phase.

V ₁₀ represents the voltage for 10% transmittance (viewed from an angle perpendicular to the substrate surface). t _on and t _off
Represents the switch-on time and the switch-off time at an operating voltage corresponding to 2.5 times the value of V ₁₀ , respectively. Δn represents the optical anisotropy, and n ₀ represents the refractive index. Δε is the dielectric anisotropy [Δε = ε‖−ε | (where ε‖
Represents the permittivity parallel to the long axis of the molecule, and ε | represents the permittivity perpendicular to it)]. Electro-optical data were measured in a TN cell at the first minimum (ie at ad · Δn value of 0.4 μ) at 20 ° C. unless otherwise indicated. Optical data were measured at 20 ° C unless otherwise indicated.

In the present application and in the examples below, the structures of liquid crystal compounds are indicated by acronyms. Therefore, conversion to the chemical formula is performed according to Tables A and B below. The radicals C _n H _{2n + 1} and C _m H _{2m + 1} are all straight-chain alkyl radicals having n or m carbon atoms, respectively. Table B
The encoding in is trivial. In Table A, only acronyms related to parent structure are shown. In each case, the parent structure acronyms are separated by hyphens, followed by the substituents R ¹ , R ² ,
The signs for L ¹ and L ² are added. That is, when replacing the symbol in each example with a chemical structure, first of all,
Reference is made to Table B in which specific structures are described, and those not listed therein are Table A and substituents R ¹ , R ² in front of Table A,
By referring to the tables for L ¹ and L ^2, the chemical structural formulas corresponding to the symbols can be obtained.

[0099]

[Table 3] The compounds listed below are especially R²And / or X is
F, Cl, CF₃, OCF ₃Or OCHF₂Is the main
It is a preferred ingredient for light media.

[0100]

[Chemical 27]

[0101]

[Chemical 28]

[0102]

[Chemical 29]

[0103]

[Chemical 30]

[0104]

[Chemical 31]

[0105]

[Table 4]

[0106]

[Table 5]

[0107]

[Table 6]

[0108]

[Table 7]

[0109]

[Table 8]

[0110]

[Table 9]

[0111]

[Table 10]

[0112]

[Table 11]

[0113]

[Table 12]

[0114]

[Table 13]

[0115]

[Table 14]

[0116]

[Table 15]

[0117]

[Table 16]

[0118]

[Table 17]

[0119]

[Table 18]

[0120]

[Table 19]

[0121]

[Table 20]

[0122]

[Table 21]

[0123]

[Table 22]

[0124]

[Table 23]

[0125]

[Table 24]

[0126]

[Table 25]

[0127]

[Table 26]

[0128]

[Table 27]

[0129]

[Table 28]

[0130]

[Table 29]

[0131]

[Table 30]

[0132]

[Table 31]

[0133]

[Table 32]

[0134]

[Table 33]

[0135]

[Table 34]

[0136]

[Table 35]

[0137]

[Table 36]

[0138]

[Table 37]

[0139]

[Table 38]

[0140]

[Table 39]

[0141]

[Table 40]

[0142]

[Table 41]

[0143]

[Table 42]

[0144]

[Table 43]

[0145]

[Table 44]

[0146]

[Table 45]

[0147]

[Table 46]

Another example of the medium of the present invention will be shown below.

[0149]

[Table 47]

[0150]

[Table 48]

[0151]

[Table 49]

[0152]

[Table 50]

[0153]

[Table 51]

[0154]

[Table 52]

[0155]

[Table 53]

[0156]

[Table 54]

[0157]

[Table 55]

[0158]

[Table 56]

[0159]

[Table 57]

[0160]

[Table 58]

[0161]

[Table 59]

[0162]

[Table 60]

[0163]

[Table 61]

[0164]

[Table 62]

[0165]

[Table 63]

[0166]

[Table 64]

[0167]

[Table 65]

[0168]

[Table 66]

[0169]

[Table 67]

[0170]

[Table 68]

[0171]

[Table 69]

[0172]

[Table 70]

[0173]

[Table 71]

[0174]

[Table 72]

[0175]

[Table 73]

[0176]

[Table 74]

[0177]

[Table 75]

[0178]

[Table 76]

[0179]

[Table 77]

[0180]

[Table 78]

[0181]

[Table 79]

[0182]

[Table 80]

[0183]

[Table 81]

[0184]

[Table 82]

[0185]

[Table 83]

[0186]

[Table 84]

[0187]

[Table 85]

[0188]

[Table 86]

[0189]

[Table 87]

[0190]

[Table 88]

[0191]

[Table 89]

[0192]

[Table 90]

[0193]

[Table 91]

[0194]

[Table 92]

[0195]

[Table 93]

[0196]

[Table 94]

[0197]

[Table 95]

[0198]

[Table 96]

[0199]

[Table 97]

[0200]

[Table 98]

   ─────────────────────────────────────────────────── ─── Continued front page    (71) Applicant 591032596             Frankfurter Str. 250,             D-64293 Darmstadt, Fed             eral Republish of Ge             rmany (72) Inventor Herbert Prague             Federal Republic of Germany V-6100 Darm             Stadt Wingerzberg Stra             5 (72) Inventor Ulrich Finkenzeler             Federal Republic of Germany V-6831 Plan             Kustatt Waldtop Art 74 (72) Inventor Volker Reifenrad             Federal Republic of Germany V-6101 Rothed             Ruff Jahnstrasse 15 (72) Inventor Aike Pecs             Federal Republic of Germany V-6109 Mu             Luther 6 am Buchwald 4 (72) Inventor Bernhard Rieger             Japan 227 Midori Ward, Yokohama City, Kanagawa Prefecture             2834 Otadaira, Nara Town Wacore Tamagawa Academy (72) Inventor Hiroshi Numata             Miho Town, Midori Ward, Yokohama City, Kanagawa Prefecture, Japan               1351-1 Forest Hills Miho             3-202 F-term (reference) 4H027 BB03 BB04 BC04 BD04 BD05                       BD10 CB04 CE04 CM01 CM03                       CM04 CN03 CQ04 CQ05 CR03                       CR04 CS03 CS04 CT03 CT04                       CT05 CU01 CU04 CU05 CW01                       CW03 CX01

Claims (19)

[Claims] 1. A liquid crystal medium based on a mixture of polar compounds having a positive dielectric anisotropy, having the general formula I: (In the formula, X is fluorine and ring A is trans-1,4-
One or more compounds of cyclohexylene or 1,4-phenylene, and R is alkyl, oxaalkyl, fluoroalkyl or alkenyl, each having up to 7 carbon atoms, and Formulas V-VI: (Wherein, R is alkyl, oxaalkyl, fluoroalkyl or alkenyl having up to 7 carbon atoms in each case, Z is _{-C 2 H 4 -, - CO} -O- or -O-CO- 1) selected from the group consisting of
A liquid crystal medium containing one or more compounds. 2. This medium further has the following conditions (1) to (1).
2. The method according to claim 1, wherein any one of (6) is satisfied.
The liquid crystal medium described. (1) This medium contains at least one compound of the following formula II-2. [Chemical 3] Where each group has the following meanings: R: alkyl, oxaalkyl, fluoroalkyl or alkenyl having in each case up to 7 carbon atoms, X: OCF ₃ , Y: H or F, A : Trans-1,4-cyclohexylene, r: 1) (2) The medium contains two or more compounds of formula I. (3) At the first transmission minimum of Gooch and Tarry, d
The threshold voltage of the liquid crystal medium of the TN cell with Δn of 0.4 μm is 1.99 V or less. (4) This medium is the compound of formula I wherein ring A is trans-1,
Include at least one compound which is 4-cyclohexylene and at least one compound in which ring A in formula I is 1,4-phenylene. (5) This medium has general formula III-101 and formula IV
Includes one or more compounds selected from the group consisting of compounds represented by -101. [Chemical 4] (Among the above formulas III-101 and Formula IV-101, X is OCF _3; R is an alkyl having up to 7 carbon atoms in each case, oxaalkyl, fluoroalkyl or alkenyl; Q is, -C ₂ H ₄ −, −C ₄ H ₈
-Or -CO-O-; Y is H or F; A is trans-1,4-cyclohexylene or 1,4-phenylene; r is 0 or 1, respectively. (6) This medium has the general formula II-102, III-10.
2 and one or more compounds selected from the group consisting of compounds represented by IV-102. [Chemical 5] (The above formulas II-102, III-102 and IV-1
Among 02, X is Cl, CF ₃ or OCHF _2; R is an alkyl having up to 7 carbon atoms in each case, oxaalkyl, fluoroalkyl or alkenyl; Q is -
_{C 2 H 4 -, - C} 4 H 8 - or -CO-O-; Y is H or F; A is trans-1,4-cyclohexylene or 1,4-phenylene; r is 0 or 1 Respectively. ) 3. The concentration of the compound of formula I in the liquid crystal medium is 25.
The medium according to claim 1 or 2, wherein the content is at least wt%. 4. The concentration of the compound of formula I in the liquid crystal medium is 40.
The medium according to claim 1 or 2, wherein the content is at least wt%. 5. The concentration of the compound of formula I in the liquid crystal medium is 10
3 to 50% by weight.
The described medium. 6. The threshold voltage of the medium of a TN cell having a d.Δn of 0.4 μm at the first minimum transmission of Gooch and Tarry is 1.8 V or less. The medium according to any one. 7. The medium according to claim 6, wherein the threshold voltage is 1.6 volts or less. 8. The medium of claim 6, wherein the threshold voltage is 1.4 to 1.6 volts. 9. R in the formula I shown in claim 1 is C ₂
-C _{7-1E-alkenyl,} C ₄ -C ₇ -3E- alkenyl or C ₅ -C ₇ -4- medium of claim 1, wherein the alkenyl, compound characterized in that it comprises one or more. 10. R in formula I as shown in claim 1 is vinyl, 1E-propenyl, 1E-butenyl, 1E-pentenyl, 1E-hexenyl, 1E-heptenyl, 3-butenyl, 3E-pentenyl, 3E-. Hexenyl, 3E-
Heptenyl, 4-pentenyl, 4Z-hexenyl, 4E
Medium according to claim 9, characterized in that it is -hexenyl or 4Z-heptenyl. 11. General formulas II-5, III-5 and I
V-5: (Wherein, each group has the following meanings: R: alkyl having up to 7 carbon atoms in each case, oxaalkyl, fluoroalkyl or _{alkenyl; Q: -C 2 H 4 -} , - C 4 H ₈ - or -CO-O-, X: F, Cl, CF 3, OCF 3 or OCHF _2, Y: H or F, A: trans-1,4-cyclohexylene or 1,4
A medium according to any one of claims 1 to 10, characterized in that it further comprises one or more compounds selected from the group consisting of phenylene, r: 0 or 1). (However, in this medium, in formula II-2, III-101,
IV-101, II-102, III-102 or I
When the compound represented by V-102 is present, the compound which is not the same as those compounds is represented by the general formulas II-5 and II.
It is selected as a compound represented by I-5 and IV-5. ) 12. The formula II-5, III-5, wherein the medium is a linear alkenyl in which R has 2 to 7 carbon atoms.
The medium according to claim 11, which comprises one or more compounds selected from the group of: and IV-5. 13. The compound of the general formula V and the general formula V
Z is -C in I ₂H_FourFrom the group consisting of compounds
To contain one or more compounds selected
The medium according to any one of claims 1 to 12, which is characterized. 14. General formulas VII to XII: Wherein R, r, X and Y are each independently of the other as defined in claim 11 and further comprises one or more compounds selected from the group The medium according to any one of claims 1 to 13. 15. A compound of formulas I-IV in all mixtures, wherein the compound of formula II is a compound of formula II-2, II-102 or II-5,
The compound of formula I is a compound represented by any of formulas III-101, III-102 and III-5.
Compounds of V are those of formulas IV-101, IV-102 and I
It is a compound represented by any of V-5. The medium according to any one of claims 1 to 13, characterized in that the combined proportions of) are at least 50% by weight. 16. The proportion of the compounds of the formulas II to IV (wherein the compounds of the formulas II to IV have the same meaning as defined in claim 15) in the whole mixture is 30 to 70% by weight. The medium according to any one of claims 1 to 15, characterized in that: 17. A medium according to claim 1, which consists essentially of a compound selected from the group consisting of the general formulas I to XII. 18. An electro-optical device using the liquid crystal medium according to claim 1. 19. An electro-optical liquid crystal display containing the liquid crystal medium according to claim 1.